Protein sequencing methods and reagents

Abstract

Described are optical methods and reagents for sequencing polypeptides. A probe that exhibits different spectral properties when conjugated to different N-terminal amino acids is conjugated to the N-terminal amino acid of a polypeptide. Sequentially detecting one or more spectral properties of the probe conjugated to the N-terminal amino acid and cleaving the N-terminal amino acid produces sequence information of the polypeptide. The use of super-resolution microscopy allows for the massively parallel sequencing of individual polypeptide molecules in situ such as within a cell. Also described are probes comprising hydroxymethyl rhodamine green, an isothiocyanate group and a protecting group.

Description

RELATED APPLICATIONS[0001]This application claims the benefit of priority of U.S. Provisional Patent Application No. 62 / 242,619 filed Oct. 16, 2015, the contents of which are hereby incorporated by reference.FIELD OF THE INVENTION[0002]This invention relates to the field of protein sequencing and more specifically to methods, assays and reagents for sequencing protein or polypeptide molecules as well as to fluorescent single molecule imaging methods, assays and reagents for sequencing individual polypeptide molecules.BACKGROUND OF THE INVENTION[0003]Proteins underlie virtually every biological process; perturbations in their expression, degradation, interactions, or localization are associated with disease. Yet while methods for protein identification, quantification and imaging are needed throughout biomedicine, existing techniques have serious constraints.[0004]Historically (1960-90s), protein sequencing was based on Edman degradation, which involves the sequential chemical modifi...

AI Technical Summary

Benefits of technology

The patent describes a probe that uses a fluorescent dye to detect and locate proteins within cells. The dye can be attached to a specific protein or can be designed to bind to a specific part of the protein. The probe can also be used in optical detection with super-resolution microscopy. Additionally, the probe can be designed to facilitate the chemical cleavage of a specific amino acid from the protein. Overall, this technology can help researchers better understand how proteins function in cells and may also have potential applications in drug development.

Problems solved by technology

Yet while methods for protein identification, quantification and imaging are needed throughout biomedicine, existing techniques have serious constraints.

While automatable, the technology has low sensitivity and is not applicable to heterogeneous samples (i.e. mixtures of different polypeptides), limiting utility.

Yet it also suffers from limited dynamic range, biased detection, and incremental performance gains.

Moreover, it is based on ensemble measurements (bulk analysis), resulting in the loss of valuable contextual information (e.g. protein subcellular localization etc.).

Crucially, however, these methods depend on the availability of fluorescent antibodies, or other similarly labeled affinity capture reagents such as aptamers, which are physically large relative to most cellular polypeptides, diminishing resolution, and / or which may bind cellular proteins in addition to the target of interest, producing artifacts, and typically fewer than 3-4 different cellular proteins can be imaged together at one time.

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